Canonical Allele Identifier: CA361490912
Gene: PURA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114681T>A , CM000667.2:g.140114681T>A GRCh38
NC_000005.9:g.139494266T>A , CM000667.1:g.139494266T>A GRCh37
NC_000005.8:g.139474450T>A NCBI36
NG_041813.1:g.5559T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.500T>A MANE Select ENSP00000332706.3:p.Phe167Tyr
ENST00000651386.1:c.500T>A ENSP00000499133.1:p.Phe167Tyr
ENST00000331327.4:c.500T>A ENSP00000332706.3:p.Phe167Tyr
NM_005859.4:c.500T>A NP_005850.1:p.Phe167Tyr
NM_005859.5:c.500T>A MANE Select NP_005850.1:p.Phe167Tyr